SAS Programmer I

PSI CRO; Buenos Aires; Presencial; ARS 1.200.000 - 2.400.000; Jornada completa

Descripción de la vacante

PSI CRO in Argentina seeks a skilled statistical programmer to contribute to global clinical trials. You will work with international teams of statisticians, programmers and data managers, programming data sets and summaries.

You will develop analysis data sets, write SAS programs for ADS and Tables, Listings and Figures, support validations and prepare documentation for regulatory submissions.

Formación

• University and Master’s degree in applied science, mathematics, statistics or the like.
• Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system is desirable.
• Good knowledge of programming logic, SQL and macro programming is preferred.
• Proficient in English, spoken and written.
• Experience within clinical trials and/or Biostatistics.
• Good analytical skills and MS Office proficiency.
• Excellent communication and interpersonal skills.

Responsabilidades

• Develop analysis data sets structure for global clinical trials.
• Develop program requirements and specifications for analyses.
• Be involved in SAS programming of ADS and Tables, Listings and Figures.
• Support SAS program validations and maintain documentation.
• Produce Tables, Listings and Figures and communicate with project teams.

Conocimientos

SAS programming

SQL

Macro programming

English

Analytical skills

Communication skills

Educación

Master's degree in statistics or applied science

Herramientas

SAS Base/STAT/GRAPH

Descripción del empleo

We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do.A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

You willcontribute to statistical programming activities related to global clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets andsummaries.

You will:

• Develop analysis data sets structure
• Develop program requirements and specifications
• Be involved in SAS programming of ADS and Tables, Listings and Figures
• Support SAS program validations
• Prepareand review program documentation
• Produce TFL
• Communicatewith project teams and company departments with regard to statistical programming of clinical research projects

Qualifications

• UniversityandMaster's degree in applied science, mathematics, statistics or the like
• Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system is desirable
• Good knowledge of programming logic, SQL and macro programming is preferred
• Proficient inEnglish, spoken and written
• Experience within clinical trials and/or Biostatistics
• Good analytical skills
• Proficiency in standard MS Office applications
• Excellent communication and interpersonal skills

Additional Information

Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors.Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.